Wang Xiaoguang, Rundle Charles H, Wergedal Jon E, Srivastava Apurva K, Mohan Subburaman, Lau K-H William
Musculoskeletal Disease Center (151), J. L. Pettis Memorial Veterans Administration Medical Center, 11201 Benton Street, Loma Linda, CA 92357, USA.
Calcif Tissue Int. 2007 Jun;80(6):374-82. doi: 10.1007/s00223-007-9026-0. Epub 2007 May 23.
Sex-dependent differences were identified in the femoral bone parameters of male and female ob/ob (leptin knockout) mice compared with their C57BL/6 wild-type background strain. Total fat, lean weight and body weight were not different between adult male and female leptin knockout mice. However, leptin knockout males exhibited lower lean weights than C57BL/6 males. Peripheral quantitative computerized tomographic measurements at the femoral midshaft revealed that the normal differences in the periosteal circumference, endosteal circumference, total bone mineral content, and polar moment of inertia normally observed between adult male and female wild-type mice were lost between adult male and female ob/ob mice. Significant reductions in these bone parameters were seen in male ob/ob mice compared to male wild-type mice but not in female ob/ob mice compared to female wild-type mice. In prepubertal mice, there were no differences in phenotype and femoral bone parameters between males and females within any strain, suggesting sex hormone functions. Serum free testosterone levels were 5.6-fold higher in adult male ob/ob mice than in adult male C57BL/6 wild-type mice, and serum estradiol levels were 1.8- and 1.3-fold greater in adult male and female ob/ob mice, respectively, than in their wild-type counterparts. Androgen receptor gene expression was not different in femur-derived bone cells of male ob/ob mice compared with wild-type mice. The loss of sex-related differences in these bone parameters in adult male ob/ob mice might result from deficient signaling in the androgen signaling pathway and the fact that leptin functions are permissive for androgen effects on bone development.
与C57BL/6野生型背景品系相比,在雄性和雌性ob/ob(瘦素基因敲除)小鼠的股骨参数中发现了性别依赖性差异。成年雄性和雌性瘦素基因敲除小鼠的总脂肪、瘦体重和体重没有差异。然而,瘦素基因敲除的雄性小鼠的瘦体重低于C57BL/6雄性小鼠。股骨中轴的外周定量计算机断层扫描测量显示,成年雄性和雌性野生型小鼠之间通常观察到的骨膜周长、骨内膜周长、总骨矿物质含量和极惯性矩的正常差异在成年雄性和雌性ob/ob小鼠之间消失了。与雄性野生型小鼠相比,雄性ob/ob小鼠的这些骨参数显著降低,但与雌性野生型小鼠相比,雌性ob/ob小鼠没有这种情况。在青春期前的小鼠中,任何品系的雄性和雌性在表型和股骨骨参数上没有差异,提示性激素的作用。成年雄性ob/ob小鼠的血清游离睾酮水平比成年雄性C57BL/6野生型小鼠高5.6倍,成年雄性和雌性ob/ob小鼠的血清雌二醇水平分别比其野生型对应物高1.8倍和1.3倍。与野生型小鼠相比,雄性ob/ob小鼠股骨来源的骨细胞中的雄激素受体基因表达没有差异。成年雄性ob/ob小鼠这些骨参数中性别相关差异的丧失可能是由于雄激素信号通路中的信号缺陷,以及瘦素功能对雄激素对骨骼发育的影响具有允许作用这一事实。